
Last Updated: 09/26/2026
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Found 58 publications
Bi-allelic missense variants in human GPN2 result in Perrault syndrome.
Journal: American journal of human genetics
Published: March 27, 2026
The development of inner ear gene therapy for DFNB9: From bench to bedside.
Journal: Hearing research
Published: December 24, 2025
Predictors of postoperative gustatory disturbance and gustatory recovery following microsurgical resection of vestibular schwannoma.
Journal: Journal of neuro-oncology
Published: November 16, 2025
The relationship between extent of resection, tumor recurrence, and facial nerve outcomes in vestibular schwannoma surgery: a single-institution experience and systematic review.
Journal: Journal of neuro-oncology
Published: September 11, 2025
International expert consensus on gene therapy for hereditary hearing loss: Based on clinical trials.
Journal: Med (New York, N.Y.)
Published: July 22, 2025
SLC26A4-AP-2 mu2 interaction regulates SLC26A4 plasma membrane abundance in the endolymphatic sac.
Journal: Science advances
Published: October 09, 2024
AAV-mediated inner ear gene delivery triggers mild host immune responses in the mammalian inner ear.
AAV-mediated inner ear gene delivery triggers mild host immune responses in the mammalian inner ear.
Journal: Molecular therapy. Methods & clinical development
Published: September 10, 2024
Interaction between the TBC1D24 TLDc domain and the KIBRA C2 domain is disrupted by two epilepsy-associated TBC1D24 missense variants.
Journal: The Journal of biological chemistry
Published: March 27, 2024
Dual-AAV vector-mediated expression of MYO7A improves vestibular function in a mouse model of Usher syndrome 1B.
Journal: Molecular therapy. Methods & clinical development
Published: March 14, 2023
Combined AAV-mediated gene replacement therapy improves auditory function in a mouse model of human DFNB42 deafness.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: February 08, 2023
Last Updated: 09/26/2026